Literature DB >> 25648836

Comprehensive spectroscopic characterization of finasteride polymorphic forms. Does the form X exist?

Jadwiga Frelek1, Marcin Górecki, Alicja Dziedzic, Ewa Jabłońska, Bohdan Kamieński, Ryszard K Wojcieszczyk, Roman Luboradzki, Wojciech J Szczepek.   

Abstract

The pure polymorphic forms I, II, and III of finasteride were prepared and their purity was confirmed by FTIR, differential scanning calorimetry, and X-ray powder diffraction measurements. The preparation experiments demonstrated that the desolvation process of some finasteride solvates does result not only in the formation of polymorphic forms I and II, but also in obtaining the pure form III. The (13)C cross-polarization magic angle spinning (CP-MAS) and the (15)N CP-MAS spectra can distinguish all three polymorphic forms of finasteride. Additionally, the data point to the presence of only one molecule in crystallographic asymmetric unit of polymorphic forms I and III and two molecules in the form II. The application of electronic circular dichroism (ECD) and vibrational circular dichroism (VCD) spectroscopy for finasteride polymorphic forms shows that the three polymorphs could be distinguished by the characteristic shapes of their VCD spectra in the spectral range 1520-1440 cm(-1). The ECD spectral patterns of all these forms, however, are almost indistinguishable because of their close similarity. Comparison of the (13)C CP-MAS spectra of forms I, II, and III with those reported in the literature indicates that the so-called finasteride "form X" is identical to the previously known finasteride form III. On this basis, the existence of form X was excluded.
© 2015 Wiley Periodicals, Inc. and the American Pharmacists Association.

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Keywords:  Calorimetry (DSC); FTIR (Fourier transform infrared spectroscopy); X-ray powder diffractometry; chirality; circular dichroism; finasteride; polymorphism; solid-state NMR

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Year:  2015        PMID: 25648836     DOI: 10.1002/jps.24369

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  1 in total

1.  Steroidal Molecular Rotors with 1,4-Diethynylphenylene Rotators: Experimental and Theoretical Investigations Toward Seeking Efficient Properties.

Authors:  Karolina Olszewska; Izabella Jastrzebska; Andrzej Łapiński; Marcin Górecki; Rosa Santillan; Norberto Farfán; Tomasz Runka
Journal:  J Phys Chem B       Date:  2020-10-16       Impact factor: 2.991

  1 in total

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